Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1805092 | 0.925 | 0.080 | 1 | 65570758 | missense variant | A/G | snv | 2 | |||
rs806381 | 0.925 | 0.080 | 6 | 88156182 | intron variant | A/G | snv | 0.32 | 2 | ||
rs10822184 | 1.000 | 10 | 63577393 | intron variant | T/C;G | snv | 2 | ||||
rs8179206 | 1.000 | 2 | 27497575 | missense variant | A/G | snv | 1.9E-03 | 7.2E-04 | 1 |